Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10780607	0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10868018	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12343646	0.92[EUR][1000 genomes]
rs3860931	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3860935	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3860936	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs3860937	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3860939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3860943	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4097647	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs4097648	0.85[AMR][1000 genomes]
rs4120051	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4877778	0.91[EUR][1000 genomes]
rs4877779	0.92[EUR][1000 genomes]
rs4877782	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6559730	0.85[ASN][1000 genomes]
rs6559731	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7035629	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7863524	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7873385	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893512	chr9:86022215-86323309	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1038884	chr9:86089963-86215800	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86105600-86107800	Enhancers	Fetal Heart	heart
2	chr9:86106200-86107800	Enhancers	Left Ventricle	heart
3	chr9:86106200-86107800	Enhancers	NHDF-Ad	bronchial
4	chr9:86106200-86108000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:86106400-86107600	Enhancers	Spleen	Spleen
6	chr9:86106400-86108000	Enhancers	Psoas Muscle	Psoas
7	chr9:86106400-86108000	Enhancers	Right Ventricle	heart
8	chr9:86106600-86107600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr9:86107000-86108200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr9:86107200-86107800	Enhancers	Right Atrium	heart
11	chr9:86107200-86115200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:86107200-86123000	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr9:86107400-86107600	Enhancers	Ovary	ovary
14	chr9:86107400-86108800	Weak transcription	Hela-S3	cervix

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